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HOXB13 mutations and binding partners in prostate development and cancer: Function, clinical significance, and future directions
A prospective study of dietary and supplemental zinc intake and risk of type 2 diabetes depending on genetic variation in SLC30A8
TNF receptors 1 and 2 exert distinct region‐specific effects on striatal and hippocampal grey matter volumes (VBM) in healthy adults
Variants in the CNR1 gene predispose to headache with nausea in the presence of life stress
Additional Evidence Supports Association of Common Variants in COL11A1 with Increased Risk of Hip Osteoarthritis Susceptibility
Dopamine receptors genes polymorphisms in Parkinson patients with levodopa-induced dyskinesia
MDR1 and CYP3A4 genes variants association with clinical response measured on a five-factor model in multiepisodic schizophrenia and related …
Association between prolactin gene polymorphism (–1149 G/T) and hyperprolactinemia in anti-psychotic treated patients with schizophrenia
Genetic 3′ UTR variation is associated with human pigmentation characteristics and sensitivity to sunlight
Genetic diversity of 71 Y-chromosomal biallelic markers in the Han population living in Southern China